Package 69367-184-08

Brand: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride

Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-184-08
Digits Only 6936718408
Product NDC 69367-184
Description

240 mL in 1 BOTTLE (69367-184-08)

Marketing

Marketing Status
Marketed Since 2018-03-15
Brand dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Generic dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bb61a68-58fa-45ed-b9e8-4a5f83f7046b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0369367184083"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1429362"], "spl_set_id": ["a58bfb14-28f9-4425-a5a5-aaff4847c979"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (69367-184-08)", "package_ndc": "69367-184-08", "marketing_start_date": "20180315"}], "brand_name": "DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE", "product_id": "69367-184_4bb61a68-58fa-45ed-b9e8-4a5f83f7046b", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "69367-184", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "18 mg/15mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/15mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180315", "listing_expiration_date": "20261231"}